IMMUNIZATION OF MELANOMA PATIENTS WITH GANGLIOSIDES
Project Number5R01CA040532-02
Contact PI/Project LeaderLIVINGSTON, PHILIP O.
Awardee OrganizationSLOAN-KETTERING INST CAN RESEARCH
Description
Abstract Text
Three cell surface antigens expressed on melanomas are now available in
purified form, the gangliosides GD2, GD3 and GM2. All three serve as
differentiation antigens for different subsets of cells of neuroectodermal
lineage. Both GD2 and GM2 are known to be potentially immunogenic in man
as they have been identified by a variety of human sera. The clinical
relevance of GD3 has been demonstrated by inflammatory reactions and major
clinical responses in 3 melanoma patients treated with anti-GD3 monoclonal
antibody (R24). We have however, been unable to develop consistently
immunogenic vaccines in man or in the mouse using whole cells or cell
lysates expressing these gangliosides. Consequently, we have explored the
effect of purified GM2 and GD2 vaccines in the mouse and have identified
approaches that consistently induce an antibody response. The success of
these murine trials has encouraged us to proceed with similar trials in
Stage II melanoma patients. In our initial 3 trials, none of 6 patients
immunized with GM2 alone produced antibody but 5 of 11 patients immunized
with GM2 plus BCG or GM2 plus Salmonella minn. mutant R595 have produced
antibody reactive with GM2 (median titer 320). These sera mediate
complement dependent cytotoxicity on human melanoma and astrocytoma cells
with human complement. ITLC confirmed that they react exclusively with
GM2. The approaches proposed here are (and will continue to be) based on
the results of these ongoing studies in the mouse. In intitial trials we
will change the dose, schedule and route of administration of GM2 plus BCG
or R595 or both to further increase the anti GM2 response rate. Subsequent
trials will test other vaccines such as liposomes containing GM2 and GM2
covalently attached to BSA or KLH. Stage II melanoma patients will be
vaccinated after, or before and after, lymphadenectomy in small groups and
their serological reactivity and delayed hypersensitivity reactions to the
relevant gangliosides tested. The immunized lymph nodes removed at surgery
will be used to produce human monoclonal antibodies. Approaches provoking
a consistent serological or DTH responses will be used with GD2 and GD3,
and subsequently with the three gangliosides together. Vaccines producing
a consistent response in Stage II patients will be used in patients with
measurable disease to gauge their effect on immune responses in the face of
more advanced disease.
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